A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3685355



Internal ID18983636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:21917803..22009451hg38UCSC Ensembl
Innerchr8:21775314..21866962hg19UCSC Ensembl
Innerchr8:21831260..21922908hg18UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3891649
hg1991649
hg1891649
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1018546
Supporting Variants
Samples
Known GenesXPO7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3685355
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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